ES2197594T3 - Procedimiento para el tratamiento de materiales textiles. - Google Patents

Procedimiento para el tratamiento de materiales textiles.

Info

Publication number: ES2197594T3
Authority: ES; Spain
Prior art keywords: alkyl; formula; branched; linear; hydrogen
Prior art date: 1998-04-06
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

ES99810266T

Other languages

English (en)

Spanish (es)

Inventor

Frank Bachmann

Josef Dannacher

Cornelia Makowka

Gunther Schlingloff

Peter Weingartner

Grit Richter

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF Schweiz AG

Original Assignee

Ciba Spezialitaetenchemie Holding AG

Ciba SC Holding AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-04-06

Filing date

1999-03-29

Publication date

2004-01-01

1999-03-29 Application filed by Ciba Spezialitaetenchemie Holding AG, Ciba SC Holding AG filed Critical Ciba Spezialitaetenchemie Holding AG

2004-01-01 Application granted granted Critical

2004-01-01 Publication of ES2197594T3 publication Critical patent/ES2197594T3/es

2019-03-29 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 31
239000000463 material Substances 0.000 title description 9
239000004753 textile Substances 0.000 title description 5
239000003599 detergent Substances 0.000 claims abstract description 28
150000002978 peroxides Chemical class 0.000 claims abstract description 16
125000003118 aryl group Chemical group 0.000 claims description 57
125000000217 alkyl group Chemical group 0.000 claims description 48
229910052739 hydrogen Inorganic materials 0.000 claims description 37
239000001257 hydrogen Substances 0.000 claims description 37
150000001875 compounds Chemical class 0.000 claims description 31
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 29
239000000975 dye Substances 0.000 claims description 21
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 19
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 15
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 13
239000011572 manganese Substances 0.000 claims description 13
125000004093 cyano group Chemical group *C#N 0.000 claims description 12
229910052736 halogen Inorganic materials 0.000 claims description 11
150000002367 halogens Chemical class 0.000 claims description 11
229910052748 manganese Inorganic materials 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
101100516563 Caenorhabditis elegans nhr-6 gene Proteins 0.000 claims description 8
BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 claims description 8
150000002431 hydrogen Chemical class 0.000 claims description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 7
150000001450 anions Chemical class 0.000 claims description 7
125000004429 atom Chemical group 0.000 claims description 7
125000005842 heteroatom Chemical group 0.000 claims description 6
150000002576 ketones Chemical class 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
239000002736 nonionic surfactant Substances 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 5
239000003945 anionic surfactant Substances 0.000 claims description 5
150000007942 carboxylates Chemical class 0.000 claims description 5
150000004985 diamines Chemical class 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
230000009103 reabsorption Effects 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
150000001299 aldehydes Chemical class 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
230000008569 process Effects 0.000 claims description 4
ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 4
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 3
235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 3
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 2
NJQFCQXFOHVYQJ-PMACEKPBSA-N BF 4 Chemical compound C1([C@@H]2CC(=O)C=3C(O)=C(C)C4=C(C=3O2)[C@H](C(C)C)C2=C(O4)C(C)=C(C(C2=O)(C)C)OC)=CC=CC=C1 NJQFCQXFOHVYQJ-PMACEKPBSA-N 0.000 claims description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
229910002651 NO3 Inorganic materials 0.000 claims description 2
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
150000004820 halides Chemical class 0.000 claims description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
229910052727 yttrium Inorganic materials 0.000 claims description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 3
239000001267 polyvinylpyrrolidone Substances 0.000 claims 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
239000003086 colorant Substances 0.000 abstract description 4
239000007788 liquid Substances 0.000 abstract description 4
230000008034 disappearance Effects 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 76
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 67
239000000243 solution Substances 0.000 description 62
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 61
239000000203 mixture Substances 0.000 description 28
239000003054 catalyst Substances 0.000 description 24
239000007787 solid Substances 0.000 description 23
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 21
239000003446 ligand Substances 0.000 description 21
239000000725 suspension Substances 0.000 description 20
238000004440 column chromatography Methods 0.000 description 18
238000006243 chemical reaction Methods 0.000 description 17
235000002639 sodium chloride Nutrition 0.000 description 17
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 16
239000000047 product Substances 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
239000002253 acid Substances 0.000 description 14
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
239000011780 sodium chloride Substances 0.000 description 12
239000012141 concentrate Substances 0.000 description 11
SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical group OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 11
IUNJCFABHJZSKB-UHFFFAOYSA-N 2,4-dihydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C(O)=C1 IUNJCFABHJZSKB-UHFFFAOYSA-N 0.000 description 10
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 10
235000008504 concentrate Nutrition 0.000 description 10
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 10
230000000694 effects Effects 0.000 description 10
239000003480 eluent Substances 0.000 description 10
-1 halides Chemical class 0.000 description 10
150000002696 manganese Chemical class 0.000 description 10
239000003921 oil Substances 0.000 description 10
235000019198 oils Nutrition 0.000 description 10
238000003756 stirring Methods 0.000 description 10
CESXSDZNZGSWSP-UHFFFAOYSA-L manganese(2+);diacetate;tetrahydrate Chemical compound O.O.O.O.[Mn+2].CC([O-])=O.CC([O-])=O CESXSDZNZGSWSP-UHFFFAOYSA-L 0.000 description 9
238000010992 reflux Methods 0.000 description 9
WZUODJNEIXSNEU-UHFFFAOYSA-N 2-Hydroxy-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(O)=C1 WZUODJNEIXSNEU-UHFFFAOYSA-N 0.000 description 8
WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 description 8
239000000376 reactant Substances 0.000 description 8
239000012043 crude product Substances 0.000 description 7
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
238000004040 coloring Methods 0.000 description 6
MMIPFLVOWGHZQD-UHFFFAOYSA-N manganese(3+) Chemical compound [Mn+3] MMIPFLVOWGHZQD-UHFFFAOYSA-N 0.000 description 6
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 6
238000005406 washing Methods 0.000 description 6
244000257039 Duranta repens Species 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
239000000499 gel Substances 0.000 description 5
239000002244 precipitate Substances 0.000 description 5
238000000746 purification Methods 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
238000012360 testing method Methods 0.000 description 5
RPMOVPAOVYQKTQ-UHFFFAOYSA-N 2-[(2-amino-2-methylpropyl)iminomethyl]-5-(diethylamino)phenol Chemical compound CCN(CC)c1ccc(C=NCC(C)(C)N)c(O)c1 RPMOVPAOVYQKTQ-UHFFFAOYSA-N 0.000 description 4
QGKJJNMJGMWELK-UHFFFAOYSA-N 2-[(2-amino-2-methylpropyl)iminomethyl]-5-(dimethylamino)phenol Chemical compound CN(C)c1ccc(C=NCC(C)(C)N)c(O)c1 QGKJJNMJGMWELK-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
239000012153 distilled water Substances 0.000 description 4
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
150000004760 silicates Chemical class 0.000 description 4
MDPQZLHLSGXJHB-HZPDHXFCSA-N 2-[[(1R,2R)-2-aminocyclohexyl]iminomethyl]-5-(diethylamino)phenol Chemical compound CCN(CC)c1ccc(C=N[C@@H]2CCCC[C@H]2N)c(O)c1 MDPQZLHLSGXJHB-HZPDHXFCSA-N 0.000 description 3
ZWVHTXAYIKBMEE-UHFFFAOYSA-N 2-hydroxyacetophenone Chemical compound OCC(=O)C1=CC=CC=C1 ZWVHTXAYIKBMEE-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000004061 bleaching Methods 0.000 description 3
239000013078 crystal Substances 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
OPCJOXGBLDJWRM-UHFFFAOYSA-N 1,2-diamino-2-methylpropane Chemical compound CC(C)(N)CN OPCJOXGBLDJWRM-UHFFFAOYSA-N 0.000 description 2
FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 2
238000005160 1H NMR spectroscopy Methods 0.000 description 2
YALGEDKXAVVZCR-VXGBXAGGSA-N 2-[[(1R,2R)-2-aminocyclohexyl]iminomethyl]phenol Chemical compound N[C@@H]1CCCC[C@H]1N=Cc1ccccc1O YALGEDKXAVVZCR-VXGBXAGGSA-N 0.000 description 2
241001459693 Dipterocarpus zeylanicus Species 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
238000005481 NMR spectroscopy Methods 0.000 description 2
235000019502 Orange oil Nutrition 0.000 description 2
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
150000004696 coordination complex Chemical class 0.000 description 2
239000000835 fiber Substances 0.000 description 2
239000006260 foam Substances 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
238000002156 mixing Methods 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
239000010502 orange oil Substances 0.000 description 2
150000001451 organic peroxides Chemical class 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
229920005646 polycarboxylate Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
HFIYIRIMGZMCPC-YOLJWEMLSA-J remazole black-GR Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(\N=N\C=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-YOLJWEMLSA-J 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000001694 spray drying Methods 0.000 description 2
238000010186 staining Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
229940098465 tincture Drugs 0.000 description 2
238000012546 transfer Methods 0.000 description 2
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical group C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 description 1
YIYBRXKMQFDHSM-UHFFFAOYSA-N 2,2'-Dihydroxybenzophenone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1O YIYBRXKMQFDHSM-UHFFFAOYSA-N 0.000 description 1
HSMMICHYGPYAMR-UHFFFAOYSA-N 2-[(2-aminophenyl)iminomethyl]-5-(diethylamino)phenol Chemical compound CCN(CC)c1ccc(C=Nc2ccccc2N)c(O)c1 HSMMICHYGPYAMR-UHFFFAOYSA-N 0.000 description 1
NRKPWTQKZGMMEW-UHFFFAOYSA-N 2-[4-[4-(1-benzofuran-2-yl)phenyl]phenyl]-1-benzofuran Chemical group C1=CC=C2OC(C3=CC=C(C=C3)C3=CC=C(C=C3)C3=CC4=CC=CC=C4O3)=CC2=C1 NRKPWTQKZGMMEW-UHFFFAOYSA-N 0.000 description 1
XFVZSRRZZNLWBW-UHFFFAOYSA-N 4-(Diethylamino)salicylaldehyde Chemical compound CCN(CC)C1=CC=C(C=O)C(O)=C1 XFVZSRRZZNLWBW-UHFFFAOYSA-N 0.000 description 1
KURCTZNCAHYQOV-UHFFFAOYSA-N 4-(dimethylamino)-2-hydroxybenzaldehyde Chemical compound CN(C)C1=CC=C(C=O)C(O)=C1 KURCTZNCAHYQOV-UHFFFAOYSA-N 0.000 description 1
WSCKXNRHWPMWHS-FGZHOGPDSA-N 4-[[(1R,2R)-2-[[4-(diethylamino)-2-hydroxyphenyl]methylideneamino]cyclohexyl]iminomethyl]benzene-1,3-diol Chemical compound C(C)N(C=1C=C(C(C=N[C@H]2[C@@H](CCCC2)N=CC=2C(O)=CC(=CC2)O)=CC1)O)CC WSCKXNRHWPMWHS-FGZHOGPDSA-N 0.000 description 1
GTWKMYUBUXHJGC-WOJBJXKFSA-N 4-[[(1R,2R)-2-[[4-(dimethylamino)-2-hydroxyphenyl]methylideneamino]cyclohexyl]iminomethyl]benzene-1,3-diol Chemical compound CN(C)c1ccc(C=N[C@@H]2CCCC[C@H]2N=Cc2ccc(O)cc2O)c(O)c1 GTWKMYUBUXHJGC-WOJBJXKFSA-N 0.000 description 1
KBCLQLKFTDQXDD-UHFFFAOYSA-N 5-(diethylamino)-2-[2-[(2-hydroxyphenyl)methylideneamino]ethyliminomethyl]phenol Chemical compound C(C)N(C=1C=C(C(C=NCCN=CC=2C(O)=CC=CC2)=CC1)O)CC KBCLQLKFTDQXDD-UHFFFAOYSA-N 0.000 description 1
LBWYPTFEIKNIFU-DHIUTWEWSA-N 5-(diethylamino)-2-[[(1R,2R)-2-[(2-hydroxy-4-methoxyphenyl)methylideneamino]cyclohexyl]iminomethyl]phenol Chemical compound C(C)N(C=1C=C(C(C=N[C@H]2[C@@H](CCCC2)N=CC=2C(O)=CC(=CC2)OC)=CC1)O)CC LBWYPTFEIKNIFU-DHIUTWEWSA-N 0.000 description 1
LPPNDQGPJMZXEF-FGZHOGPDSA-N 5-(diethylamino)-2-[[(1R,2R)-2-[(2-hydroxyphenyl)methylideneamino]cyclohexyl]iminomethyl]phenol Chemical compound C(C)N(C=1C=C(C(C=N[C@H]2[C@@H](CCCC2)N=CC=2C(O)=CC=CC2)=CC1)O)CC LPPNDQGPJMZXEF-FGZHOGPDSA-N 0.000 description 1
NUFXZWIIXXEAMC-UHFFFAOYSA-N 5-(diethylamino)-2-[[2-[(2-hydroxyphenyl)methylideneamino]phenyl]iminomethyl]phenol Chemical compound C(C)N(C=1C=C(C(C=NC2=C(C=CC=C2)N=CC=2C(O)=CC=CC2)=CC1)O)CC NUFXZWIIXXEAMC-UHFFFAOYSA-N 0.000 description 1
NYNCIJQTBCFJNZ-WOJBJXKFSA-N 5-(dimethylamino)-2-[[(1R,2R)-2-[(2-hydroxyphenyl)methylideneamino]cyclohexyl]iminomethyl]phenol Chemical compound CN(C=1C=C(C(C=N[C@H]2[C@@H](CCCC2)N=CC=2C(O)=CC=CC2)=CC1)O)C NYNCIJQTBCFJNZ-WOJBJXKFSA-N 0.000 description 1
CFNMUZCFSDMZPQ-GHXNOFRVSA-N 7-[(z)-3-methyl-4-(4-methyl-5-oxo-2h-furan-2-yl)but-2-enoxy]chromen-2-one Chemical compound C=1C=C2C=CC(=O)OC2=CC=1OC/C=C(/C)CC1OC(=O)C(C)=C1 CFNMUZCFSDMZPQ-GHXNOFRVSA-N 0.000 description 1
239000004382 Amylase Substances 0.000 description 1
102000013142 Amylases Human genes 0.000 description 1
108010065511 Amylases Proteins 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
229940120146 EDTMP Drugs 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
101100114416 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) con-10 gene Proteins 0.000 description 1
240000001987 Pyrus communis Species 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
229910021536 Zeolite Inorganic materials 0.000 description 1
DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000012190 activator Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
229910052910 alkali metal silicate Inorganic materials 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
235000019418 amylase Nutrition 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
235000019568 aromas Nutrition 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
230000008859 change Effects 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
239000012230 colorless oil Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 1
238000004453 electron probe microanalysis Methods 0.000 description 1
238000006735 epoxidation reaction Methods 0.000 description 1
UFZOPKFMKMAWLU-UHFFFAOYSA-N ethoxy(methyl)phosphinic acid Chemical compound CCOP(C)(O)=O UFZOPKFMKMAWLU-UHFFFAOYSA-N 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
239000010931 gold Substances 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000005469 granulation Methods 0.000 description 1
235000012907 honey Nutrition 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
KQFUCKFHODLIAZ-UHFFFAOYSA-N manganese Chemical compound [Mn].[Mn] KQFUCKFHODLIAZ-UHFFFAOYSA-N 0.000 description 1
150000002697 manganese compounds Chemical class 0.000 description 1
CSPLVMZJCALKHX-UHFFFAOYSA-N manganese(2+);tetrahydrate Chemical compound O.O.O.O.[Mn+2] CSPLVMZJCALKHX-UHFFFAOYSA-N 0.000 description 1
239000002808 molecular sieve Substances 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000004967 organic peroxy acids Chemical class 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
239000000049 pigment Substances 0.000 description 1
125000004193 piperazinyl group Chemical group 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003219 pyrazolines Chemical class 0.000 description 1
KUIXZSYWBHSYCN-UHFFFAOYSA-L remazol brilliant blue r Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=C2C(=O)C3=CC=CC=C3C(=O)C2=C1NC1=CC=CC(S(=O)(=O)CCOS([O-])(=O)=O)=C1 KUIXZSYWBHSYCN-UHFFFAOYSA-L 0.000 description 1
238000010898 silica gel chromatography Methods 0.000 description 1
239000000344 soap Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
QTTDXDAWQMDLOF-UHFFFAOYSA-J tetrasodium 3-[[4-[[4-[(6-amino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]-6-sulfonatonaphthalen-1-yl]diazenyl]naphthalen-1-yl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].Nc1ccc2c(O)c(N=Nc3ccc(N=Nc4ccc(N=Nc5cc(c6cccc(c6c5)S([O-])(=O)=O)S([O-])(=O)=O)c5ccccc45)c4ccc(cc34)S([O-])(=O)=O)c(cc2c1)S([O-])(=O)=O QTTDXDAWQMDLOF-UHFFFAOYSA-J 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
230000009466 transformation Effects 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
150000003624 transition metals Chemical class 0.000 description 1
DCYIADGZPJOOFN-UHFFFAOYSA-N vat brown 1 Chemical compound C1=CC=C2C(=O)C3=CC=C4C(C5=C(C6=C7C(C8=CC=CC=C8C6=O)=O)NC6=C8C(=O)C9=CC=CC=C9C(C8=CC=C65)=O)=C7NC4=C3C(=O)C2=C1 DCYIADGZPJOOFN-UHFFFAOYSA-N 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1
239000010457 zeolite Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
- C07C251/24—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to carbon atoms of six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic Table
- C07F13/005—Compounds without a metal-carbon linkage
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0021—Dye-stain or dye-transfer inhibiting compositions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/168—Organometallic compounds or orgometallic complexes
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3932—Inorganic compounds or complexes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Inorganic Chemistry (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Photoreceptors In Electrophotography (AREA)

ES99810266T 1998-04-06 1999-03-29 Procedimiento para el tratamiento de materiales textiles. Expired - Lifetime ES2197594T3 (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP98810289		1998-04-06
EP98810289		1998-04-06

Publications (1)

Publication Number	Publication Date
ES2197594T3 true ES2197594T3 (es)	2004-01-01

Family

ID=8236022

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES99810266T Expired - Lifetime ES2197594T3 (es)	1998-04-06	1999-03-29	Procedimiento para el tratamiento de materiales textiles.

Country Status (16)

Country	Link
US (2)	US6413926B2 (zh)
EP (1)	EP0955289B1 (zh)
JP (2)	JP4290269B2 (zh)
KR (1)	KR100662217B1 (zh)
CN (1)	CN1137978C (zh)
AR (1)	AR014819A1 (zh)
AT (1)	ATE239696T1 (zh)
AU (1)	AU756053B2 (zh)
BR (1)	BR9901238A (zh)
CA (1)	CA2267847A1 (zh)
DE (1)	DE59905403D1 (zh)
DK (1)	DK0955289T3 (zh)
ES (1)	ES2197594T3 (zh)
ID (1)	ID22607A (zh)
PT (1)	PT955289E (zh)
TW (1)	TW408203B (zh)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1159259A1 (en) *	1999-03-08	2001-12-05	Ciba SC Holding AG	Manganese complexes of salen ligands and the use thereof
KR20020085775A (ko)	1999-03-08	2002-11-16	시바 스페셜티 케미칼스 홀딩 인크.	직물 재료의 처리 방법
AU2002216760A1 (en)	2000-07-05	2002-01-14	Ciba Specialty Chemicals Holding Inc.	Process for the preparation of manganese complexes of salen compounds
WO2004065302A2 (en)	2003-01-24	2004-08-05	Ciba Specialty Chemicals Holding Inc.	Crystalline modification of a manganese complex
US8404628B1 (en) *	2008-12-08	2013-03-26	Hbi Branded Apparel Enterprises, Llc	Method for spray bleaching cellulosic fabrics
EP3382004A1 (en)	2017-03-28	2018-10-03	Basf Se	Acylhydrazone granules for use in laundry detergents

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK0521099T3 (da) *	1990-03-21	1998-09-07	Res Corp Technologies Inc	Chirale katalysatorer og epoxidationsreaktioner katalyseret derved
AT397509B (de) *	1992-08-03	1994-04-25	Loba Feinchemie Aktiengesellsc	Zusatzstoff für mineralöle und mineralölprodukte, speziell elektroisolieröle
US5696109A (en) *	1992-12-07	1997-12-09	Eukarion, Inc.	Synthetic catalytic free radical scavengers useful as antioxidants for prevention and therapy of disease
DE69412188T2 (de) *	1993-06-19	1999-03-11	Ciba Specialty Chemicals Holding Inc., Basel	Inhibierung der Wiederabsorption von migrierenden Farbstoffen in der Waschlösung
JP3801626B2 (ja) *	1994-02-04	2006-07-26	スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー	プロキラルなオレフィンのエポキシ化法およびそのエポキシ化に用いる触媒ならびにその触媒を調製するための中間体
DE69533149T2 (de) *	1994-07-21	2005-08-25	Ciba Specialty Chemicals Holding Inc.	Bleichmittelzusammensetzung für Gewebe
GB9425296D0 (en) *	1994-12-15	1995-02-15	Ciba Geigy Ag	Inhibition of dye migration
DE19529905A1 (de) *	1995-08-15	1997-02-20	Henkel Kgaa	Aktivatorkomplexe für Persauerstoffverbindungen
GB9523654D0 (en) *	1995-11-18	1996-01-17	Ciba Geigy Ag	Fabric bleaching composition
EP0902083B1 (en) *	1997-09-09	2004-10-13	Ciba SC Holding AG	Fabric care method

1999
- 1999-03-16 TW TW088104022A patent/TW408203B/zh not_active IP Right Cessation
- 1999-03-29 AT AT99810266T patent/ATE239696T1/de not_active IP Right Cessation
- 1999-03-29 DE DE59905403T patent/DE59905403D1/de not_active Expired - Lifetime
- 1999-03-29 ES ES99810266T patent/ES2197594T3/es not_active Expired - Lifetime
- 1999-03-29 PT PT99810266T patent/PT955289E/pt unknown
- 1999-03-29 EP EP99810266A patent/EP0955289B1/de not_active Expired - Lifetime
- 1999-03-29 DK DK99810266T patent/DK0955289T3/da active
- 1999-03-30 JP JP08733299A patent/JP4290269B2/ja not_active Expired - Fee Related
- 1999-03-31 AU AU22571/99A patent/AU756053B2/en not_active Ceased
- 1999-04-01 CA CA002267847A patent/CA2267847A1/en not_active Abandoned
- 1999-04-05 CN CNB991048113A patent/CN1137978C/zh not_active Expired - Fee Related
- 1999-04-05 AR ARP990101517A patent/AR014819A1/es not_active Application Discontinuation
- 1999-04-05 ID IDP990303A patent/ID22607A/id unknown
- 1999-04-05 BR BR9901238-3A patent/BR9901238A/pt not_active Application Discontinuation
- 1999-04-06 KR KR1019990011850A patent/KR100662217B1/ko not_active IP Right Cessation
2001
- 2001-04-13 US US09/835,245 patent/US6413926B2/en not_active Expired - Fee Related
2002
- 2002-05-07 US US10/140,530 patent/US6737391B2/en not_active Expired - Fee Related
2008
- 2008-09-22 JP JP2008242113A patent/JP2009067796A/ja not_active Withdrawn

Also Published As

Publication number	Publication date
EP0955289A3 (de)	1999-12-01
ID22607A (id)	1999-12-02
CA2267847A1 (en)	1999-10-06
US20020183228A1 (en)	2002-12-05
ATE239696T1 (de)	2003-05-15
JP2009067796A (ja)	2009-04-02
EP0955289B1 (de)	2003-05-07
US6737391B2 (en)	2004-05-18
KR19990082953A (ko)	1999-11-25
CN1231330A (zh)	1999-10-13
PT955289E (pt)	2003-09-30
BR9901238A (pt)	2000-05-30
DE59905403D1 (de)	2003-06-12
DK0955289T3 (da)	2003-09-01
JP4290269B2 (ja)	2009-07-01
AU2257199A (en)	1999-10-14
JP2000054256A (ja)	2000-02-22
CN1137978C (zh)	2004-02-11
AR014819A1 (es)	2001-03-28
AU756053B2 (en)	2003-01-02
US6413926B2 (en)	2002-07-02
EP0955289A2 (de)	1999-11-10
KR100662217B1 (ko)	2007-01-02
TW408203B (en)	2000-10-11
US20010023238A1 (en)	2001-09-20

Publication	Publication Date	Title
ES2255503T3 (es)	2006-07-01	Complejos metalicos de ligandos tripodales.
KR100352540B1 (ko)	2002-10-31	세척액중 이동성 염료의 재흡수 억제방법
JPH0867687A (ja)	1996-03-12	布地漂白組成物
AU751675B2 (en)	2002-08-22	Fabric care method
JPH08231987A (ja)	1996-09-10	移染の防止方法
ES2197594T3 (es)	2004-01-01	Procedimiento para el tratamiento de materiales textiles.
JP2000500518A (ja)	2000-01-18	繊維漂白組成物
ES2215627T3 (es)	2004-10-16	Proceso de lavado y limpieza.
KR20160111397A (ko)	2016-09-26	세탁용 세제 중의 광표백제로서의 오르토-치환된 에톡실화 Al 또는 Zn-프탈로시아닌 화합물의 용도
EP1159259A1 (en)	2001-12-05	Manganese complexes of salen ligands and the use thereof
MXPA99003156A (en)	2000-10-01	Method of treatment of textiles
MXPA98007313A (en)	1999-09-20	Method for caring for te